T16T (p.Thr16Thr) variant of CSRP3 (P50461)
T16T (p.Thr16Thr) in CSRP3 (P50461) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
T16T (p.Thr16Thr) variant details
- p.Thr16Thr
- gnomAD 11-19192401-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0841
- CADD 0.49
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available